Location: Home-based in Melbourne (preferred) or Sydney
What you will be doing:
- Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock.
- You will be embedded in our client’s study team and have a dedicated line manager to support you
- Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports
You are:
- Degree in Pharmacy or any related course
- Min. 2+ years prior monitoring experience in a CRO/ pharmaceutcial or Biotech company
- Excellent communication skills
- Excellent knowledge of international guidelines ICH-GCP, good knowledge of local regulations
- Flexibility to travelÂ
Apply here: https://careers.iconplc.com/job/senior-clinical-research-associate-in-melbourne-sydney-jid-36022